HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41612508C= , CM000679.2:g.41612508C= | GRCh38 |
NC_000017.10:g.39768760C= , CM000679.1:g.39768760C= | GRCh37 |
NC_000017.9:g.37022286C= | NCBI36 |
NG_008301.1:g.5320G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301653.9:c.181G= MANE Select | ENSP00000301653.3:p.Ala61= | |
ENST00000301653.8:c.181G= | ENSP00000301653.3:p.Ala61= | |
ENST00000588319.1:n.258G= | ||
ENST00000593067.1:c.-312-222G= | ENSP00000467124.1:n.-312-222G= | |
NM_005557.3:c.181G= | NP_005548.2:p.Ala61= | |
NM_005557.4:c.181G= MANE Select | NP_005548.2:p.Ala61= |